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Novel Ag 2 O nanoparticles modified MoS 2 nanoflowers for piezoelectric-assisted full solar spectrum photocatalysis
The separation of photoinduced electrons and holes can enhance the photocatalytic properties of photocatalysts. A piezoelectric field is created inside piezoelectric materials, such as ZnO and MoS , by applying strain. The electrons and holes become separated under the driving force of the piezoelec...
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Published in: | Journal of colloid and interface science 2019-03, Vol.537, p.206 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | The separation of photoinduced electrons and holes can enhance the photocatalytic properties of photocatalysts. A piezoelectric field is created inside piezoelectric materials, such as ZnO and MoS
, by applying strain. The electrons and holes become separated under the driving force of the piezoelectric field. Here, we propose combining piezoelectric MoS
nanoflowers (NFs) and full solar response Ag
O nanoparticles (NPs) to form a MoS
@Ag
O heterostructure and achieve high efficiency full solar (UV, visible, and near-infrared) photocatalysis. Under both full solar light and ultrasonic excitation, the MoS
@Ag
O heterostructures can rapidly degrade methyl orange (MO) in aqueous solution. A built-in electric field is formed by the spontaneous polarization potential of the MoS
NFs during this process, and an ultrasonic wave as a driving force can consecutively change the potential created by the piezoelectric effect. Under light irradiation, electrons and holes are generated in the Ag
O NPs, and the photogenerated electrons and holes with opposite signs in the two Ag
O NPs at the two surfaces of the MoS
NFs, can be separated respectively, along the spontaneous polarized direction. Therefore, the piezoelectric effect-induced enhancement of carrier separation under ultrasonic excitation can improve the full solar photocatalytic performance of the MoS
@Ag
O heterostructures. |
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ISSN: | 1095-7103 |
DOI: | 10.1016/j.jcis.2018.11.013 |